California Quality Engineering Analyst

To support a regulated medical device environment, the contract Quality Engineering Analyst will track complaints, evaluate quality data, and collaborate with cross-functional teams to ensure compliance and improve product quality. Key responsibilities Track and trend complaints and quality data while evaluating medical and non-medical complaints Support root cause investigations and CAPA activities, documenting findings for FDA/ISO compliance Analyze data to identify risks and develop reports and dashboards for stakeholders Required qualifications Bachelor's Degree in Biomedical Engineering, Engineering, or a related field Experience in medical device, pharmaceutical, or FDA/ISO-regulated environments Knowledge of CAPA and root cause investigation processes Strong skills in Microsoft Excel and quality data analysis Experience with quality systems and complaint databases